Package 51862-571-30

Brand: Doxycycline Hyclate

Generic: Doxycycline Hyclate
NDC Package

Package Facts

Identity

Package NDC 51862-571-30
Digits Only 5186257130
Product NDC 51862-571
Product ID 51862-571_add48643-bcf3-4426-b9c1-06fa82b27b78
Description

30 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-571-30)

Marketing

Marketing Status
Marketed Since 2020-10-02
Brand Doxycycline Hyclate
Generic Doxycycline Hyclate
Sample Package No

Linked Drug Pages (1)

Doxycycline Hyclate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "add48643-bcf3-4426-b9c1-06fa82b27b78", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1653433", "2122343"], "spl_set_id": ["f9c63af9-d613-43fc-b8e5-ab6219f24c70"], "manufacturer_name": ["Mayne Pharma Commercial LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-571-30)", "package_ndc": "51862-571-30", "marketing_start_date": "20201002"}], "brand_name": "Doxycycline Hyclate", "product_id": "51862-571_add48643-bcf3-4426-b9c1-06fa82b27b78", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "51862-571", "generic_name": "Doxycycline Hyclate", "labeler_name": "Mayne Pharma Commercial LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "80 mg/1"}], "application_number": "NDA050795", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20201002", "listing_expiration_date": "20261231"}